Veeda Lifescience Hiring Fresher for Medical Writer Role

ByPharma Hiring Hub

Veeda Lifescience, a global clinical research organization, is hiring for the role of Medical Writer at its Ahmedabad location. This opportunity is ideal for B.Pharm and M.Pharm graduates with 0–2 years of experience who are looking to build a career in medical writing, scientific documentation, and clinical research communication.

The role focuses on supporting clinical documents, regulatory‑related content, scientific reports, and medical communication deliverables within a structured and quality‑driven environment. Candidates will work closely with cross‑functional teams to ensure accurate, compliant, and well‑structured medical content.

This position offers a strong entry‑level opportunity to develop long‑term expertise in medical writing and clinical documentation within a globally regulated CRO setting.

Veeda lifescience Medical writer role

Job Overview

  • Position: Medical Writer
  • Department: Medical writing
  • Location: Ahmedabad
  • Experience: 0 to 2 Years
  • Qualification: B.Pharm, M.Pharm
  • Job Type: Full-Time
  • Last Date of application: Not provided

Key Responsibilities – Medical Writer

  • Study Document Preparation & Review: Prepare and review clinical study documents including Protocols, Informed Consent Documents (ICD), Study Synopses, and other study‑specific materials such as patient diary cards.
  • Investigator Brochure (IB): Prepare and review Investigator Brochures in accordance with regulatory and sponsor requirements.
  • Clinical Trial Feasibility Support: Support preliminary and detailed trial feasibility assessments for patient‑based clinical studies in coordination with the medical team for regulatory submissions.
  • Literature Search & Background Review: Perform reference literature searches and reviews to support assigned clinical and regulatory projects.
  • Protocol Training: Provide protocol training to monitors and site teams as required.
  • Clinical Study Reports (CSR): Prepare and review Clinical Study Reports (CSRs) for various trial phases conducted by the Clinical Operations team.
  • Define CSR timelines in the project execution grid in coordination with the Project Manager.
  • CSR Variants & Interim Reports: Prepare and review full CSRs, abbreviated CSRs, synoptic CSRs, CSR shells, and interim reports as per sponsor requirements.
  • CTD / eCTD Submission Support: Finalize CSRs and related appendices for submission as part of CTD/eCTD dossiers, ensuring regulatory compliance.
  • Statistical Document Review: Review Statistical Analysis Plans (SAPs), mock shells, and Table/Figure/Listing (TFL) specifications for content accuracy and consistency.
  • Audit & Inspection Readiness: Support sponsor audits and regulatory inspections (e.g., US FDA, EMA, DCGI) and prepare responses to queries or deficiencies.
  • Documentation Quality & Compliance: Ensure high‑quality writing, editing, and presentation of clinical documentation, maintaining compliance with internal standards and external regulatory guidelines.
  • SOP Development & Review: Prepare and review departmental SOPs and contribute to cross‑departmental SOP updates as required.
  • Archiving & Documentation Control: Ensure timely archiving/e‑archiving of reports, appendices, and related documents.
  • Reporting & Project Summaries: Prepare project summaries and submit reports to the reporting head or designated stakeholders.
  • Templates & Formatting Standards: Develop and maintain document templates, formats, and styles to meet industry, internal, client, and regulatory requirements.
  • Process Improvement & Training:Participate in departmental and interdepartmental process improvement initiatives and training programs.

Required Skills & Qualifications

  • Educational Qualification
    • Degree in Life Sciences or related healthcare disciplines.
    • Required qualifications include B.Pharmacy or M.Pharmacy.
  • Experience
    • Experience in medical writing, clinical research, or regulatory documentation is preferred.
    • Freshers with strong scientific writing skills and sound clinical knowledge may also be considered.
  • Scientific Writing & Editing: Strong ability to write, edit, and review scientific and clinical documents with clarity and accuracy.
  • Clinical & Regulatory Knowledge
    • Good understanding of clinical trial processes, Clinical Study Reports (CSRs), and regulatory submission requirements.
    • Familiarity with ICH guidelines and global regulatory standards.
  • Attention to Detail: High level of accuracy and consistency in document preparation and review.
  • Communication & Collaboration: Effective communication skills with the ability to collaborate across cross‑functional clinical and regulatory teams.

Why Join Veeda Lifescience

  • Strong Foundation in Medical Writing
  • Gain hands‑on experience in protocols, CSRs, Investigator Brochures, regulatory documents, and clinical trial communications within a regulated environment.
  • Excellent Opportunity for Freshers
  • Veeda offers a supportive platform for freshers and early‑career professionals to start and grow their careers in medical writing and clinical documentation.
  • Regulatory & Compliance Exposure
  • Work on documents aligned with ICH guidelines, CTD/eCTD submissions, and global regulatory requirements, strengthening your regulatory writing skills.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ – Medical Writer

1. Who can apply for the Medical Writer role at Veeda Lifescience?

Candidates with a B.Pharmacy or M.Pharmacy degree in Life Sciences or related healthcare disciplines can apply.

2. Is this role suitable for freshers?

Yes. Freshers with strong scientific writing skills and good clinical knowledge are encouraged to apply. Candidates with up to 2 years of experience in medical writing or clinical research are also suitable.

3. What type of documents will I work on in this role?

You will work on Protocols, Informed Consent Documents (ICDs), Investigator Brochures, Clinical Study Reports (CSRs), summaries, and other regulatory‑related clinical documents.

4. Will I be involved in Clinical Study Report (CSR) writing?

Yes. The role includes preparation and review of Full CSRs, Abbreviated CSRs, Synoptic CSRs, interim reports, shells, and related appendices.

5. Does the role involve regulatory submission support?

Yes. You will contribute to CTD/eCTD submission documents, ensuring compliance with ICH guidelines and global regulatory requirements.

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